Label: ANTICOAGULANT CITRATE DEXTROSE (ACD-A)- dextrose monohydrate, sodium citrate, unspecified form, and citric acid monohydrate solution
- NDC Code(s): 14537-820-00, 14537-820-01, 14537-820-03
- Packager: Terumo BCT, Ltd
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated July 25, 2023
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HIGHLIGHTS OF PRESCRIBING INFORMATION
These highlights do not include all the information needed to use ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A safely and effectively. See full prescribing information for ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A.
ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A
Sterile Fluid
Polyolefin Container (solution bag)
Clear Overwrap
Initial U.S. Approval: 2012INDICATIONS AND USAGE
ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A is an anticoagulant intended for use only with devices that prepare Platelet Rich Plasma (PRP) products for extracorporeal use. See the device operator's manual for additional information and complete usage instructions. (1)
DOSAGE AND ADMINISTRATION
- ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A is added to blood products collected for extracorporeal processing. (2)
- ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A may only be used with devices that prepare Platelet Rich Plasma (PRP) products for extracorporeal use. For instructions on the use of the solution see the device operator's manual. (2.1)
- Follow the directions for drawing ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A into a syringe for further processing of the collected blood product. (2.2)
DOSAGE FORMS AND STRENGTHS
- 50 mL sterile fluid in a polyolefin solution bag. (3)
CONTRAINDICATIONS
- NOT FOR PREPARATION OF BLOOD PRODUCTS FOR TRANSFUSION OR FOR DIRECT INTRAVENOUS INFUSION. (4)
WARNINGS AND PRECAUTIONS
- Do not use the ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A unless the solution is clear and the container is intact and undamaged. Use aseptic technique throughout all procedures to ensure donor safety and quality. (5)
ADVERSE REACTIONS
Citrate reactions or toxicity may occur with the injection of blood products containing citrate anticoagulant. The recipient of the blood product containing citrate should be monitored for the signs and symptoms of citrate toxicity. (6)
To report SUSPECTED ADVERSE REACTIONS, contact Terumo BCT, Inc. at 1-877-339-4228 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
USE IN SPECIFIC POPULATIONS
ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A has not been studied in controlled clinical trials with specific populations. (7)
Revised: 7/2023
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Table of Contents
FULL PRESCRIBING INFORMATION: CONTENTS*
1 INDICATIONS AND USAGE
2 DOSAGE AND ADMINISTRATION
2.1 General Dosing Information
2.2 Administration
3 DOSAGE FORMS AND STRENGTHS
4 CONTRAINDICATIONS
5 WARNINGS AND PRECAUTIONS
6 ADVERSE REACTIONS
8 USE IN SPECIFIC POPULATIONS
11 DESCRIPTION
12 CLINICAL PHARMACOLOGY
12.1 Mechanism of Action
16 HOW SUPPLIED/STORAGE AND HANDLING
- *
- Sections or subsections omitted from the full prescribing information are not listed.
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1 INDICATIONS AND USAGE
ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A is an anticoagulant intended for use only with devices that prepare Platelet Rich Plasma (PRP) products for extracorporeal use. [See Dosage and Administration (2).]
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2 DOSAGE AND ADMINISTRATION
2.1 General Dosing Information
ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A is added to blood products collected for extracorporeal processing. The solution is manually added to collected blood products to facilitate extracorporeal processing. The amount of solution added is specified by the manufacturer of the processing set. It is not intended for direct intravenous infusion.
For instructions on the use of the solution with the processing set, see the device operator's manual.
2.2 Administration
- Ensure solution is the ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A and is within the expiration date.
- Inspect the solution bag. Do not use if the solution bag is damaged, leaking or if there is any visible sign of deterioration.
- Use only if solution is clear and free of particulate matter.
- Protect from sharp objects.
Directions for drawing the ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A from the solution bag.
When directed by the processing set instructions and device operator's manual:
- Open the foil pouch containing the solution by finding the notch in the foil overwrap and pulling down to present the clear overwrapped solution bag.
- Open the clear overwrap material by holding the peelable tabs between your thumb and forefinger. Gently pull the peelable tabs along the top to open the overwrap at both corners. Once both corners are opened, gently peel along the length of the overwrap. Do not place the ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A solution bag into the sterile field. The clear overwrap is not considered a sterile barrier.
- Before use, perform the following checks [see Warnings and Precautions (5)]:
- Check for leaks by gently squeezing the bag. If leaks are found, discard the solution bag.
- Ensure that the solution is the ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A and is within the expiration date.
- Inspect the solution in adequate light. Solution showing cloudiness, haze, or particulate matter should not be used.
- Aseptically prepare the Needleless Access Valve (NAV).
- Using an appropriate syringe and luer, connect to the NAV.
- Draw into the syringe the amount of ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A required by the processing set instructions and device operator's manual.
- Remove the syringe from the NAV and proceed according to the processing set instructions and device operator's manual.
Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and solution bag permit.
- 3 DOSAGE FORMS AND STRENGTHS
- 4 CONTRAINDICATIONS
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5 WARNINGS AND PRECAUTIONS
- Do not use the ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A unless the solution is clear and the container is intact and undamaged.
- Do not transfer the solution bag directly into the sterile field.
- Do not reuse. Discard unused or partially used solution bags.
- Discard the product if the Needleless Access Valve (NAV) does not function as intended.
- Aseptically prepare the NAV before use.
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6 ADVERSE REACTIONS
Citrate reactions or toxicity may occur with the injection of blood products containing citrate anticoagulant. The recipient of the blood product containing citrate should be monitored for the signs and symptoms of citrate toxicity. The signs and symptoms of citrate toxicity begin with paresthesia, a "tingling" sensation around the mouth or in the extremities, followed by severe reactions that are characterized by hypotension and possible cardiac arrhythmia. Citrate toxicity may occur more frequently in patients who are hypothermic, have impaired liver or renal function, or have low calcium levels because of an underlying disease.
- 8 USE IN SPECIFIC POPULATIONS
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11 DESCRIPTION
ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A is designed to be added to blood products collected for extracorporeal processing, to prevent platelet activation and coagulation as blood moves throughout the extracorporeal processing set.
The content of the solution bag is considered sterile. This product has a sterile fluid path only. The clear overwrap is not considered a sterile barrier. The solution is non-pyrogenic, and it contains no bacteriostatic or antimicrobial agents.
The formulas of the active ingredients are provided in Table 1.
Table 1: Active Ingredients Ingredients Molecular Formula Molecular Weight (%w/v) Citric Acid, Monohydrate C6H8O7 192.12 Dextrose Monohydrate C6H12O6 ∙ H2O 198.17 Sodium Citrate Dihydrate C6H9Na3O9 294.10 Water for Injection H2O 18.00 Each 100 mL of ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A contains: (%w/v) Citric Acid, Monohydrate 0.8 g; Dextrose Monohydrate 2.45 g; Sodium Citrate Dihydrate 2.2 g; and Water for Injection.
The solution bag is not made with natural rubber latex or PVC.
The solution bag is made from a polyolefin film. It contains materials that have been tested to demonstrate the suitability of the solution bag for storing pharmaceutical solutions. The solution contact layer is a polyolefin. The solution bag is nontoxic and biologically inert. The solution bag is a closed system and is not dependent upon entry of external air during administration. The solution bag is covered with a clear overwrap to provide protection from the physical environment. The content of the solution bag is considered sterile. This product has a sterile fluid path only. The clear overwrap is not considered a sterile barrier.
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12 CLINICAL PHARMACOLOGY
12.1 Mechanism of Action
ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A acts as an extracorporeal anticoagulant by binding the free calcium in the blood. Calcium is a necessary co-factor to several steps in the clotting cascade. The following ingredients are key components of the solution:
- Citric acid for pH regulation
- Sodium Citrate anticoagulates
- Dextrose for isotonicity
This solution has no pharmacological effect.
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16 HOW SUPPLIED/STORAGE AND HANDLING
ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A is a clear sterile solution supplied in non-pyrogenic polyolefin solution bags. Each solution bag is individually wrapped in a clear overwrap. Each clear overwrap is then individually foil wrapped. Neither the clear overwrap nor the foil overwrap can be considered a sterile barrier. This product has a sterile fluid pathway only.
SIZE CATALOG NUMBER NDC NUMBER 50 mL 40820 Case: 14537-820-03 Foil: 14537-820-01 Bag: 14537-820-00 - SPL UNCLASSIFIED SECTION
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PRINCIPAL DISPLAY PANEL - 50 mL Bag Pouch Case Label
Anticoagulant Citrate Dextrose Solution USP (ACD) Solution A
Catalog # 40820
Polyolefin Bag
50 X 50 mLNDC 14537-820-03
Indications for use: Anticoagulant intended for use only with devices that prepare Platelet
Rich Plasma (PRP) products for extracorporeal use. See Operator's Manuals for additional
information and complete usage instructions.Caution: Only the solution bag fluid path is sterile and non-pyrogenic. Do not use
unless the solution is clear and the container is intact and undamaged. Do not transfer
solution bag directly into the sterile field. Sterilized with Steam. Rx only. Single use
container. Not for preparation of blood products for transfusion or for direct intravenous
infusion.Storage Conditions:
Room temperature (68° to 77°F, 20° to 25°C).
Avoid excessive heat. Protect from freezing. Protect from direct sunlight.Each 10mL contains:
Citric Acid Monohydrate USP
0.08 g
Sodium Citrate Dihydrate USP
0.220 g
Dextrose Monohydrate USP
0.245 g
In Water for Injection USP
STERILEManufactured by TERUMO BCT, INC.
10811 West Collins Ave., Lakewood, Colorado 80215-4440, USA
Made in UK
LPN - 1000041011Lot
Expiry Date
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INGREDIENTS AND APPEARANCE
ANTICOAGULANT CITRATE DEXTROSE (ACD-A)
dextrose monohydrate, sodium citrate, unspecified form, and citric acid monohydrate solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:14537-820 Route of Administration INTRAVENOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Dextrose Monohydrate (UNII: LX22YL083G) (Anhydrous Dextrose - UNII:5SL0G7R0OK) Dextrose Monohydrate 0.245 g in 10 mL Sodium Citrate, Unspecified Form (UNII: 1Q73Q2JULR) (Sodium Cation - UNII:LYR4M0NH37) Sodium Citrate, Unspecified Form 0.220 g in 10 mL Citric Acid Monohydrate (UNII: 2968PHW8QP) (Anhydrous Citric Acid - UNII:XF417D3PSL) Anhydrous Citric Acid 0.08 g in 10 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:14537-820-03 50 in 1 CASE 1 NDC:14537-820-01 1 in 1 POUCH 1 NDC:14537-820-00 50 mL in 1 BAG; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product) Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA BA110057 07/18/2023 Labeler - Terumo BCT, Ltd (233649834) Registrant - Terumo BCT, Inc. (801679200) Establishment Name Address ID/FEI Business Operations Terumo BCT, Ltd 233649834 LABEL(14537-820) , ANALYSIS(14537-820) , STERILIZE(14537-820) , MANUFACTURE(14537-820)